| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188974346-188974568 | Rare:61; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189007882-189008142 | Rare:82; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):15 | ||||
| chr2:189441053-189441444 | Common:2; Rare:108 | ||||
| chr2:189783965-189784115 | Common:3; Rare:56; Clinvar (benign):1 | ||||
| chr2:189784275-189784537 | Common:4; Rare:94; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343893-190343931 | Rare:4 | ||||
| chr2:190534696-190534907 | Common:1; Rare:66 | ||||
| chr2:190648708-190648912 | Common:1; Rare:75 | ||||
| chr2:190880621-190880897 | Common:4; Rare:94 | ||||
| chr2:191014143-191014357 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191246173-191246353 | Common:1; Rare:44 | ||||
| chr2:191677856-191678218 | Common:4; Rare:102 | ||||
| chr2:197434981-197435192 | Rare:70 | ||||
| chr2:197453242-197453560 | Rare:108 | ||||
| chr2:197499815-197500439 | Common:1; Rare:242; Clinvar:1; Clinvar (benign):1 |